Canonical Allele Identifier: CA2580602588
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.34032049A>C , CM000675.2:g.34032049A>C GRCh38
NC_000013.10:g.34606186A>C , CM000675.1:g.34606186A>C GRCh37
NC_000013.9:g.33504186A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001749817.1:n.1515T>G